Deutsches Herzzentrum der Technischen Universität München, München, Germany.
Br J Clin Pharmacol. 2011 Oct;72(4):547-52. doi: 10.1111/j.1365-2125.2011.03960.x.
Initiation of blood coagulation occurs mainly through tissue factor (TF) that becomes exposed to blood following vascular injury. Cell-associated TF binds to the serine protease FVIIa and initiates a cascade of amplified zymogen activation reactions leading to thrombus formation. As TF-FVIIa directed inhibitors might achieve anticoagulant efficacy without significantly interfering with normal haemostasis, the TF-FVIIa complex is an interesting target in thrombosis-related disease. Various approaches have been used to inhibit the TF-FVIIa complex including active site-inhibited FVIIa, TF antibodies, tissue factor pathway inhibitor (TFPI), naturally occurring inhibitors, peptide exosite inhibitors and active site inhibitors. Several experimental studies using these inhibitors have displayed promise. However, none of these TF/FVIIa inhibitors has reached clinical testing. Further studies are required to evaluate the clinical efficacy of these novel inhibitors.
凝血的启动主要通过组织因子(TF)来实现,当血管损伤时,TF 会暴露于血液中。细胞相关的 TF 与丝氨酸蛋白酶 FVIIa 结合,启动级联放大的酶原激活反应,导致血栓形成。由于 TF-FVIIa 定向抑制剂可能在不显著干扰正常止血的情况下实现抗凝疗效,因此 TF-FVIIa 复合物是血栓形成相关疾病的一个有趣靶点。已经使用了各种方法来抑制 TF-FVIIa 复合物,包括活性位点抑制的 FVIIa、TF 抗体、组织因子途径抑制剂(TFPI)、天然抑制剂、肽外切位点抑制剂和活性位点抑制剂。使用这些抑制剂的一些实验研究显示出了希望。然而,这些 TF/FVIIa 抑制剂中没有一种已经进入临床测试。需要进一步的研究来评估这些新型抑制剂的临床疗效。